A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220301



Internal ID20787341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148859927..148864618hg38UCSC Ensembl
chr7:148557019..148561710hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg384692
hg194692
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419861
Supporting Variants
Samples
Known GenesEZH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220301
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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